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首页> 外文期刊>Environmental microbiology >Expression of a putative nitrite reductase and the reversible inhibition of nitrite-dependent respiration by nitric oxide in Nitrobacter winogradskyi Nb-255
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Expression of a putative nitrite reductase and the reversible inhibition of nitrite-dependent respiration by nitric oxide in Nitrobacter winogradskyi Nb-255

机译:亚硝酸盐杆菌Nb-255中亚硝酸还原酶的表达及一氧化氮对亚硝酸盐依赖呼吸的可逆抑制

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The nitrite oxidizing Alphaproteobacterium, Nitrobacter winogradskyi, primarily conserves energy from the oxidation of nitrite (NO2- ) to nitrate (NO3- ) through aerobic respiration. Almost 20 years ago, NO-dependent NADH formation was reported to occur in both aerobic and anaerobic cell suspensions of N. winogradskyi strain 'agilis', suggesting that NO oxidation might contribute to energy conservation by Nitrobacter. Recently, the N. winogradskyi Nb-255 genome was found to contain a gene (Nwin_2648) that encodes a putative copper-containing nitrite reductase (NirK), which may reduce NO2- to NO. In this study, the putative nirK was found to be maximally transcribed under low O-2 (between zero and 4% O-2) in the presence of NO2- . Transcription of nirK was not detected under anaerobic conditions in the absence of NO2- or in the presence of NO3- and pyruvate. Although net production of NO could not be detected from either aerobically grown or anaerobically incubated cells, exogenous NO was consumed by viable cells and concomitantly inhibited NO2--dependent O-2 uptake in a reversible, concentration dependent manner. Both NO2--dependent O-2 uptake and NO consumption were inhibited by 1 mM cyanide suggesting involvement of cytochrome oxidase with NO consumption. Abiotic consumption of NO was measured, yet, both the rates and kinetics of NO transformation in buffer alone, or by heat killed, or cyanide-treated cells differed from those of viable cells. In light of this new information, a modified model is proposed to explain how NirK and NO manage electron flux in Nitrobacter.
机译:亚硝酸盐氧化的阿尔法变形杆菌,硝化细菌winogradskyi,主要通过有氧呼吸来保存亚硝酸盐(NO2-)氧化为硝酸盐(NO3-)的能量。大约20年前,据报道,在Winogradskyi菌株“ agilis”的需氧和厌氧细胞悬浮液中均发生了NO依赖性NADH的形成,这表明NO氧化可能有助于硝化细菌的节能。最近,发现了温诺氏猪笼草Nb-255基因组包含一个基因(Nwin_2648),该基因编码一种推定的含铜亚硝酸盐还原酶(NirK),该酶可能会将NO2-还原为NO。在这项研究中,发现假定的nirK在存在NO2-的低O-2(介于零和4%O-2之间)下被最大转录。在缺氧条件下,不存在NO2-或存在NO3-和丙酮酸的条件下,未检测到nirK的转录。尽管从需氧培养或厌氧培养的细胞中均未检测到NO的净产生,但外源NO被活细胞消耗,并以可逆的浓度依赖性方式抑制了NO2依赖性O-2的吸收。 1 mM氰化物抑制了NO2依赖性O-2的吸收和NO的消耗,表明细胞色素氧化酶与NO的消耗有关。测量了NO的非生物消耗,然而,仅在缓冲液中,或通过热杀死或氰化物处理的细胞中NO转化的速率和动力学都不同于活细胞。根据这一新信息,提出了一种改进的模型来解释NirK和NO如何控制硝化细菌中的电子通量。

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